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3-[[4-(4-Iodophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine is a pyrrolopyridine derivative with the molecular formula C21H21IN4. It features a piperazine ring substituted with an iodophenyl group, which contributes to its unique chemical structure and potential pharmacological properties. 3-[[4-(4-Iodophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine has been investigated for its role as a ligand for various receptors and its potential application in the development of new therapeutic agents. Although its exact mechanism of action and specific biological activity are not yet fully understood, it has demonstrated promise as a candidate for further drug development and research in the pharmaceutical and medical fields.

158985-08-1

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158985-08-1 Usage

Uses

Used in Pharmaceutical Research and Development:
3-[[4-(4-Iodophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine is used as a chemical compound for the development of new therapeutic agents. Its unique structure and potential as a receptor ligand make it a valuable candidate for further research and drug development.
Used in Receptor Binding Studies:
In the field of medicinal chemistry, 3-[[4-(4-Iodophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine is used as a ligand for studying receptor binding and interactions. This helps researchers understand its potential pharmacological effects and mechanisms of action, which can contribute to the discovery of new drugs and therapies.
Used in Drug Design and Optimization:
3-[[4-(4-Iodophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine is utilized in the process of drug design and optimization. Its unique chemical features can be leveraged to modify and improve the properties of existing drugs or to design new molecules with enhanced therapeutic potential.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-[[4-(4-Iodophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine is used as a starting point for the synthesis of new compounds with potential therapeutic applications. Its structural features can be modified to explore various chemical and biological properties, leading to the development of novel drugs and pharmaceutical agents.

Check Digit Verification of cas no

The CAS Registry Mumber 158985-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,9,8 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 158985-08:
(8*1)+(7*5)+(6*8)+(5*9)+(4*8)+(3*5)+(2*0)+(1*8)=191
191 % 10 = 1
So 158985-08-1 is a valid CAS Registry Number.

158985-08-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-{[4-(4-Iodophenyl)-1-piperazinyl]methyl}-1H-pyrrolo[2,3-b]pyrid ine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:158985-08-1 SDS

158985-08-1Downstream Products

158985-08-1Relevant academic research and scientific papers

Synthesis of 3-[[4-(4-[18F] fluorophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine

Eskola, Olli,Bergman, Joergen,Lehikoinen, Pertti,Haaparanta, Merja,Groenroos, Tove,Forsback, Sarita,Solin, Olof

, p. 687 - 696 (2007/10/03)

3-[[4-(4-[18F]fluorophenyl)piperazin-1-yl]methyl] -1H-pyrrolo[2,3-b]pyridine, a candidate to image dopamine D4 receptors, was synthesised via electrophilic fluorination of a trimethylstannyl precursor with high specific radioactivity

Pyrrolo-pyridine derivatives

-

, (2008/06/13)

A class of pyrrolo[2,3-b]pyridine derivatives, substituted at the 3-position by a substituted piperazinylmethyl moiety, are antagonists of dopamine receptor subtypes within the brain, having a selective affinity for the dopamine D 4 receptor subtype over other dopamine receptor subtypes, and are accordingly of benefit in the treatment and/or prevention of psychotic disorders such as schizophrenia while manifesting fewer side-effects than those associated with classical neuroleptic drugs.

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